The following data is part of a premarket notification filed by Nordiclab Intl. with the FDA for Ria Test, Nordicalb Hpl.
| Device ID | K782099 |
| 510k Number | K782099 |
| Device Name: | RIA TEST, NORDICALB HPL |
| Classification | Radioimmunoassay, Human Placental Lactogen |
| Applicant | NORDICLAB INTL. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JMF |
| CFR Regulation Number | 862.1585 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-12-18 |
| Decision Date | 1979-01-10 |